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CYPROHEPTADINE HYDROCHLORIDE - 42291-225-10 - (CYPROHEPTADINE HYDROCHLORIDE)

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Drug Information of CYPROHEPTADINE HYDROCHLORIDE

Product NDC: 42291-225
Proprietary Name: CYPROHEPTADINE HYDROCHLORIDE
Non Proprietary Name: CYPROHEPTADINE HYDROCHLORIDE
Active Ingredient(s): 4    mg/1 & nbsp;   CYPROHEPTADINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CYPROHEPTADINE HYDROCHLORIDE

Product NDC: 42291-225
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040644
Marketing Category: ANDA
Start Marketing Date: 20100615

Package Information of CYPROHEPTADINE HYDROCHLORIDE

Package NDC: 42291-225-10
Package Description: 1000 TABLET in 1 BOTTLE (42291-225-10)

NDC Information of CYPROHEPTADINE HYDROCHLORIDE

NDC Code 42291-225-10
Proprietary Name CYPROHEPTADINE HYDROCHLORIDE
Package Description 1000 TABLET in 1 BOTTLE (42291-225-10)
Product NDC 42291-225
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CYPROHEPTADINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100615
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name CYPROHEPTADINE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of CYPROHEPTADINE HYDROCHLORIDE


General Information